Variant #0000540056 (NC_000010.10:g.55582205_55582210del, NM_033056.3:c.5287_5292del (PCDH15))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55582205_55582210del
DNA change (hg38) g.53822445_53822450del
Published as PCDH15(NM_001142763.1):c.5308_5313delGCTCCT (p.A1770_P1771del), PCDH15(NM_001142763.2):c.5308_5313delGCTCCT (p.A1770_P1771del)
ISCN -
DB-ID PCDH15_000216 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDH15 NM_033056.3 -/. - c.5287_5292del r.(?) p.(Ala1763_Pro1764del)


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